510(k) K811630 ยท LGE Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Trunnion-Bearing
KINEMATIC ROTATING HINGE TOTAL KNEE PR.
| Applicant | Howmedica Corp., Walker MI, US |
| Decision | Substantially Equivalent, Jul 1, 1981 |
| Received | Jun 9, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811630
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.